首页> 外文期刊>Human vaccines >Immunogenicity, reactogenicity and safety of three-dose primary and booster vaccination with combined diphtheria-tetanus-whole-cell pertussis-hepatitis B-reduced antigen content Haemophilus influenzae type b vaccine in Filipino children.
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Immunogenicity, reactogenicity and safety of three-dose primary and booster vaccination with combined diphtheria-tetanus-whole-cell pertussis-hepatitis B-reduced antigen content Haemophilus influenzae type b vaccine in Filipino children.

机译:三剂量初次和加强接种白喉-破伤风-全细胞百日咳-乙型肝炎联合疫苗可降低菲律宾儿童乙型流感嗜血杆菌疫苗的免疫原性,反应原性和安全性。

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To evaluate the immunogenicity, reactogenicity and safety of primary and booster vaccination with DTPw-HBVLT/Hib2.5 vaccine containing low thiomersal and reduced quantities of Hib polysaccharide (PRP).Combined DTP vaccines have high global coverage. Thus, the addition of new antigens to existing DTP vaccines is the most effective way to ensure high coverage.192 healthy infants were randomized to receive the investigational DTPw-HBVLT/Hib2.5 vaccine or licensed DTPw-HBV/Hib10 at 6, 10, 14 weeks. Immune memory to the Hib antigen was assessed through administration of plain PRP challenge at 10 months in 50% of subjects. Challenged and unchallenged subjects respectively received a DTP-HBV or DTPa-HBV/Hib booster at 15-18 months of age. Antibody responses were measured using enzyme-linked immunosorbent assay (ELISA) and reactogenicity was assessed using diary cards.One month post-primary vaccination, 100% and ≥ 93.7% of subjects in both groups had anti-PRP antibody concentrations ≥ 0.15 μg/mL and ≥ 1.0 μg/mL, respectively. Robust responses to PRP were observed after the 10 month plain PRP challenge and booster responses were observed in unchallenged subjects after the booster dose at 15-18 months of age. Post-primary and post-booster responses to the other vaccine antigens were at least as high in the DTPw-HBVLT/Hib2.5 group versus the DTPw-HBV/Hib10 group. The reactogenicity profile of the DTPw-HBVLT/Hib2.5 vaccine was acceptable.The DTPw-HBVLT/Hib2.5 combination vaccine with reduced thiomersal and Hib content had equivalent immunogenicity and tolerability versus the full standard DTPw-HBV/Hib10 vaccine. DTPw-HBVLT/Hib2.5 or DTPw-HBV/Hib10 vaccines can contribute to reducing childhood diseases through ensuring high vaccine coverage in mass vaccination programs. ClinicalTrials.gov identifiers: NCT 01061541, NCT00158808.
机译:为了评估含低硫柳汞和减少的Hib多糖(PRP)含量的DTPw-HBVLT / Hib2.5疫苗的初次和加强接种的免疫原性,反应原性和安全性。联合DTP疫苗具有较高的全球覆盖率。因此,向现有的DTP疫苗中添加新抗原是确保高覆盖率的最有效方法。192名健康婴儿被随机分配在6、10, 14周。通过在10个月内对50%的受试者进行普通PRP攻击来评估Hib抗原的免疫记忆。挑战者和未挑战者分别在15-18个月大时接受DTP-HBV或DTPa-HBV / Hib加强免疫。使用酶联免疫吸附测定(ELISA)测量抗体反应并使用日记卡评估反应原性。初次接种后一个月,两组中100%和≥93.7%的受试者的抗PRP抗体浓度≥0.15μg/ mL和≥1.0μg/ mL。在10个月的普通PRP激发后,观察到对PRP的强烈反应,在15-18个月大的增强剂量后,未挑战的受试者中观察到了增强反应。 DTPw-HBVLT / Hib2.5组与DTPw-HBV / Hib10组相比,初免后和加强后对其他疫苗抗原的应答至少相同。 DTPw-HBVLT / Hib2.5疫苗的反应原性特征是可以接受的。与完全标准的DTPw-HBV / Hib10疫苗相比,硫柳汞和Hib含量降低的DTPw-HBVLT / Hib2.5组合疫苗具有同等的免疫原性和耐受性。 DTPw-HBVLT / Hib2.5或DTPw-HBV / Hib10疫苗可通过确保大规模疫苗接种计划中的高疫苗覆盖率来减少儿童疾病。 ClinicalTrials.gov标识符:NCT 01061541,NCT00158808。

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